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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 991487Generated: October 26, 2026

Triphenylphosphine → HCID 9850079, compound

https://huagongshe.com/reaction/991487

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3,4-DimethoxyphenolHCID 16251—
Reactant1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
ReactantTert-butyl 7-[4-(4-cyanophenyl)-4-hydroxybutyl]-3,7-diazabicyclo[3.3.1]nonane-3-carboxylateHCID 11338532—
SolventDichloromethaneHCID 6344—
ProductHCID 9850079HCID 985007921%

Reaction Steps

Triphenylphosphine (1.11 g; 4.25 mmol) in 5 mL CH2Cl2 and 1,1′-(azodicarbonyl)dipiperidine (1.07 g; 4.25 mmol) in 15 mL CH2Cl2 were added to a stirred solution of 3,4-dimethoxyphenol (0.65 g; 4.25 mmol) and tert-butyl 7-[4-(4-cyanophenyl)-4-hydroxybutyl]-3,7-diazabicyclo-[3.3.1]nonane-3-carboxylate (from step (x) above; 0.85 g; 2.12 mmol). After 3 h, the precipitate was filtered off, and the filtrate concentrated. The residue was dissolved in aqueous tartaric acid (1 M; 25 mL) and the solution was washed with diethyl ether. The aqueous phase was made basic with and extracted again with diethyl ether. The organic layer from this second extraction was separated, dried (Na2SO4) and then concentrated to give the title compound in 21% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06465481B1
Source datasetuspto-grants-2002_10
ORD IDord-ed7cd55b91cc4393ba3736e2cc2d3a7f
Source noteuspto-grants-2002_10